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76911-73-4

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76911-73-4 Usage

General Description

1-(4-bromophenyl)-2,2,2-trifluoroethanol is a chemical compound with the molecular formula C8H6BrF3O. It is an organic compound that contains a bromine atom and three fluorine atoms attached to a benzene ring, as well as a hydroxyl group. 1-(4-broMophenyl)-2,2,2-trifluoroethanol is commonly used as a building block in the synthesis of pharmaceuticals and agrochemicals. It is also used as a solvent in organic reactions and as a reagent in the synthesis of other organic compounds. Additionally, it has potential applications in the field of organic electronics and materials science, due to its unique chemical structure and properties. 1-(4-broMophenyl)-2,2,2-trifluoroethanol should be handled with care, as it may pose health and environmental risks if not properly managed.

Check Digit Verification of cas no

The CAS Registry Mumber 76911-73-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,9,1 and 1 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 76911-73:
(7*7)+(6*6)+(5*9)+(4*1)+(3*1)+(2*7)+(1*3)=154
154 % 10 = 4
So 76911-73-4 is a valid CAS Registry Number.

76911-73-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-Bromophenyl)-2,2,2-trifluoroethanol

1.2 Other means of identification

Product number -
Other names 1-(4-bromo-phenyl)-2,2,2-trifluoro-ethanol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:76911-73-4 SDS

76911-73-4Downstream Products

76911-73-4Relevant articles and documents

Combined batch and continuous flow procedure to the chemo-enzymatic synthesis of biaryl moiety of Odanacatib

De Oliveira Lopes, Raquel,De Miranda, Amanda S.,Reichart, Benedikt,Glasnov, Toma,Kappe, C. Oliver,Simon, Robert C.,Kroutil, Wolfgang,Miranda, Leandro S.M.,Leal, Ivana C.R.,De Souza, Rodrigo O.M.A.

, p. 101 - 107 (2014)

The development of chemo-enzymatic reaction under continuous flow conditions is an emerging area where biotechnology and organic chemistry can joint efforts in order to develop better process. Here in we report our effort on the development of a continuou

Photochemical C-H Activation Enables Nickel-Catalyzed Olefin Dicarbofunctionalization

Campbell, Mark W.,Yuan, Mingbin,Polites, Viktor C.,Gutierrez, Osvaldo,Molander, Gary A.

supporting information, p. 3901 - 3910 (2021/04/06)

Alkenes, ethers, and alcohols account for a significant percentage of bulk reagents available to the chemistry community. The petrochemical, pharmaceutical, and agrochemical industries each consume gigagrams of these materials as fuels and solvents each year. However, the utilization of such materials as building blocks for the construction of complex small molecules is limited by the necessity of prefunctionalization to achieve chemoselective reactivity. Herein, we report the implementation of efficient, sustainable, diaryl ketone hydrogen-atom transfer (HAT) catalysis to activate native C-H bonds for multicomponent dicarbofunctionalization of alkenes. The ability to forge new carbon-carbon bonds between reagents typically viewed as commodity solvents provides a new, more atom-economic outlook for organic synthesis. Through detailed experimental and computational investigation, the critical effect of hydrogen bonding on the reactivity of this transformation was uncovered.

Process Development of Tryptophan Hydroxylase Inhibitor LX1031, a Drug Candidate for the Treatment of Irritable Bowel Syndrome

Bednarz, Mark S.,Iimura, Shinya,Kanamarlapudi, Ramanaiah C.,Lim, Ngiap-Kie,Wu, Wenxue,Yan, Jie,Zhang, Haiming,Zhao, Matthew M.

, p. 261 - 273 (2020/03/10)

Two process routes for LX1031, a tryptophan hydroxylase inhibitor for the treatment of irritable bowel syndrome, were developed. They shared the same left-hand and right-hand starting materials as well as the penultimate intermediate. The chiral center in

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